Hempel Ute, Müller Katrin, Preissler Carolin, Noack Carolin, Boxberger Sabine, Dieter Peter, Bornhäuser Martin, Wobus Manja
Institute of Physiological Chemistry, Medical Faculty Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Stem Cell Lab, Medical Clinic I, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Stem Cells Int. 2016;2016:7842191. doi: 10.1155/2016/7842191. Epub 2016 May 11.
Adult human bone marrow stromal cells (hBMSC) are important for many scientific purposes because of their multipotency, availability, and relatively easy handling. They are frequently used to study osteogenesis in vitro. Most commonly, hBMSC are isolated from bone marrow aspirates collected in clinical routine and cultured under the "aspect plastic adherence" without any further selection. Owing to the random donor population, they show a broad heterogeneity. Here, the osteogenic differentiation potential of 531 hBMSC was analyzed. The data were supplied to correlation analysis involving donor age, gender, and body mass index. hBMSC preparations were characterized as follows: (a) how many passages the osteogenic characteristics are stable in and (b) the influence of supplements and culture duration on osteogenic parameters (tissue nonspecific alkaline phosphatase (TNAP), octamer binding transcription factor 4, core-binding factor alpha-1, parathyroid hormone receptor, bone gla protein, and peroxisome proliferator-activated protein γ). The results show that no strong prediction could be made from donor data to the osteogenic differentiation potential; only the ratio of induced TNAP to endogenous TNAP could be a reliable criterion. The results give evidence that hBMSC cultures are stable until passage 7 without substantial loss of differentiation potential and that established differentiation protocols lead to osteoblast-like cells but not to fully authentic osteoblasts.
成人人类骨髓基质细胞(hBMSC)因其多能性、可获取性及相对易于操作,在许多科学研究中具有重要意义。它们常用于体外研究成骨作用。最常见的是,hBMSC从临床常规采集的骨髓抽吸物中分离出来,并在“塑料贴壁法”下培养,无需进一步筛选。由于供体人群的随机性,它们表现出广泛的异质性。在此,分析了531个hBMSC的成骨分化潜能。将数据用于涉及供体年龄、性别和体重指数的相关性分析。hBMSC制剂的特征如下:(a)成骨特性在多少代内保持稳定,以及(b)补充剂和培养持续时间对成骨参数(组织非特异性碱性磷酸酶(TNAP)、八聚体结合转录因子4、核心结合因子α-1、甲状旁腺激素受体、骨钙蛋白和过氧化物酶体增殖物激活蛋白γ)的影响。结果表明,无法根据供体数据对成骨分化潜能做出强有力的预测;只有诱导型TNAP与内源性TNAP的比率可能是一个可靠的标准。结果证明,hBMSC培养物在传代7次之前是稳定的,分化潜能没有实质性损失,并且既定的分化方案可产生类成骨细胞,但不能产生完全成熟的成骨细胞。